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Thomas Schwarzbraun

Showing results (1-10 of 22) with videos related to

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Trends in Genetics : TIG|January 15, 2008
Defining 'chromosomal instability'Jochen B Geigl, Anna C Obenauf, Thomas Schwarzbraun, et al.
Chromosoma|November 9, 2007
Persistence of DNA threads in human anaphase cells suggests late completion of sister chromatid decatenationLily Hui-Ching Wang, Thomas Schwarzbraun, Michael R Speicher, et al.
American Journal of Medical Genetics. Part A|November 2, 2011
MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndromeAmnon Zung, Erwin Petek, Bruria Ben-Zeev, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 15, 2011
Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutationChoong Yi Fong, Arndt Rolfs, Thomas Schwarzbraun, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
Further evidence for the pathogenicity of 15q24 microduplications distal to the minimal critical regionsKatharina M Roetzer, Thomas Schwarzbraun, Anna C Obenauf, et al.
Orthopaedic Surgery|February 20, 2013
Re-alignment-procedures for skeletal dysplasia in three patients with genetically diverse syndromesAli Al Kaissi, Rudolf Ganger, Katharina M Roetzer, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|January 19, 2010
Sporadic gastric Peutz-Jeghers polyp with intraepithelial neoplasiaLars Harbaum, Jochen B Geigl, Hildegard Volkholz, et al.
Journal of Human Genetics|December 21, 2005
Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC geneLisa Ofner, Jochen Raedle, Christian Windpassinger, et al.
Bone|July 6, 2010
Altered bone matrix mineralization in a patient with Rett syndromeJochen G Hofstaetter, Katharina M Roetzer, Petra Krepler, et al.
Histopathology|December 21, 2010
Androgen receptor expression in breast cancer patients tested for BRCA1 and BRCA2 mutationsGunda Pristauz, Edgar Petru, Elvira Stacher, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Trends in Genetics : TIG|January 15, 2008
Defining 'chromosomal instability'Jochen B Geigl, Anna C Obenauf, Thomas Schwarzbraun, et al.
Chromosoma|November 9, 2007
Persistence of DNA threads in human anaphase cells suggests late completion of sister chromatid decatenationLily Hui-Ching Wang, Thomas Schwarzbraun, Michael R Speicher, et al.
American Journal of Medical Genetics. Part A|November 2, 2011
MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndromeAmnon Zung, Erwin Petek, Bruria Ben-Zeev, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 15, 2011
Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutationChoong Yi Fong, Arndt Rolfs, Thomas Schwarzbraun, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
Further evidence for the pathogenicity of 15q24 microduplications distal to the minimal critical regionsKatharina M Roetzer, Thomas Schwarzbraun, Anna C Obenauf, et al.
Orthopaedic Surgery|February 20, 2013
Re-alignment-procedures for skeletal dysplasia in three patients with genetically diverse syndromesAli Al Kaissi, Rudolf Ganger, Katharina M Roetzer, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|January 19, 2010
Sporadic gastric Peutz-Jeghers polyp with intraepithelial neoplasiaLars Harbaum, Jochen B Geigl, Hildegard Volkholz, et al.
Journal of Human Genetics|December 21, 2005
Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC geneLisa Ofner, Jochen Raedle, Christian Windpassinger, et al.
Bone|July 6, 2010
Altered bone matrix mineralization in a patient with Rett syndromeJochen G Hofstaetter, Katharina M Roetzer, Petra Krepler, et al.
Histopathology|December 21, 2010
Androgen receptor expression in breast cancer patients tested for BRCA1 and BRCA2 mutationsGunda Pristauz, Edgar Petru, Elvira Stacher, et al.
Pageof 3